77177503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16758316-G-A

77177503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16758316-G-C

77177503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16758316-G-T

77177587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16758231-C-T

77177630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16758188-G-T

77177686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16758156-C-G

77177686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16758156-C-T

http://identifiers.org/hco/9/GRCh38#77177859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16758008-C-A

77177859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16758008-C-T

http://identifiers.org/hco/9/GRCh38#77177917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16757950-C-A

77177917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16757950-C-T

http://identifiers.org/hco/9/GRCh38#77178275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#16757701-A-C

77178275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, undefined
orthologous variants: 16757701-A-G

77178275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, undefined
orthologous variants: 16757701-A-T

77178366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16757623-C-T

77178388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16757602-G-T

77178433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, undefined
orthologous variants: 16757549-A-G

77178499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, undefined
orthologous variants: 16757480-C-T

77178569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16757428-G-C

77178588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16757378-C-T

77178623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16757344-A-G

77178995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16756994-A-G

77181009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16753926-C-T

77181191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16753696-G-A

77199834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16744011-T-C

77199879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16743964-A-G

77200003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16743844-T-C

77200022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16743826-T-C

77200158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16743694-A-G

77200161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16743691-G-T

77200871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16739939-G-A

77200902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16739907-T-C

77201227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16739683-A-G

http://identifiers.org/hco/9/GRCh38#77201231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16739679-A-C

77201462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16739459-A-G

http://identifiers.org/hco/9/GRCh38#77201507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16739414-C-A

77201681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16739281-C-T

77202053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16738852-T-C

77202066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16738846-T-C

77202148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16738785-A-G

77202455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16738539-A-G

77202625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16738374-A-T

77203080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737516-C-T

77203094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737502-G-A

77205244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737457-G-T

http://identifiers.org/hco/9/GRCh38#77205245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16737456-A-C

77205245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737456-A-G

77205276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737425-A-G

77205276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737425-A-T

77205425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737290-A-G

77205458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737263-T-A

77205478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737245-A-G

77205532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737183-T-C

http://identifiers.org/hco/9/GRCh38#77205534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16737181-C-A

77205534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16737181-C-T

77206132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16736922-A-G

77206209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16736845-T-A

77206413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16736726-A-G

http://identifiers.org/hco/9/GRCh38#77206822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16736342-C-A

77206822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16736342-C-G

77207059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16735874-T-A

77209191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16731967-T-G

77209301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16731834-T-C

http://identifiers.org/hco/9/GRCh38#77209449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16731697-A-C

77209449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16731697-A-G

77209465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: stop gained
orthologous variants: 16731681-T-A

http://identifiers.org/hco/9/GRCh38#77209506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16731640-A-C

77209506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16731640-A-G

http://identifiers.org/hco/9/GRCh38#77209615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16731555-C-A

77209615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731555-C-T

77209673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731506-A-G

77209846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731382-G-A

77209846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731382-G-T

http://identifiers.org/hco/9/GRCh38#77209853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16731375-A-C

77210696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729460-T-A

77210696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729460-T-C

77210764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729404-A-G

77210797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729354-T-G

http://identifiers.org/hco/9/GRCh38#77210798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16729353-C-A

77212879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16727610-T-G

77212975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16727537-G-A

http://identifiers.org/hco/9/GRCh38#77213065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16727450-A-C

77213065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16727450-A-G

77213097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16727422-A-G

77213099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16727420-A-G

77213237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16727286-A-T

77213300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16727223-T-G

77213309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16727214-T-C

77213390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16727148-T-A

77213390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16727148-T-C

http://identifiers.org/hco/9/GRCh38#77214285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16726989-C-A

77214285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16726989-C-T

77214458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16726817-A-G

77214458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16726817-A-T

77215409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725790-C-T

77215460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725747-T-A

77215488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725723-G-A

77215860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725474-A-T

77215888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725448-C-T

77215934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725422-C-G

77215953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725403-A-G

77216280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725130-A-G

77216289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725121-T-C

77216362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725063-C-G

77216386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725041-G-A

77216416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16725011-G-A

77219042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16724012-A-G

77219043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16724011-A-T

77219117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16723936-C-T

77219293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16723862-T-A

http://identifiers.org/hco/9/GRCh38#77219325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16723833-C-A

77219849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16723539-G-T

http://identifiers.org/hco/9/GRCh38#77219871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16723522-C-A

77219909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16723485-T-G

77220286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16723120-A-G

77220305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16723101-C-T

http://identifiers.org/hco/9/GRCh38#77220375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16723031-C-A

77220375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: synonymous variant
orthologous variants: 16723031-C-T

77220390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16723016-G-T

http://identifiers.org/hco/9/GRCh38#77220391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16723015-C-A

77220391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16723015-C-G

77220391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16723015-C-T

77220435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16722959-A-G

http://identifiers.org/hco/9/GRCh38#77220498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16722896-C-A

77220520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16722880-A-T

77220603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16722807-C-T

77220611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16722799-A-G

77220639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16722773-G-C

77221816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16721529-A-G

77222176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16721159-G-C

77225651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16720694-T-A

77226212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16720189-T-C

http://identifiers.org/hco/9/GRCh38#77226359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16720037-A-C

77226359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16720037-A-T

77226422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719974-A-G

77226616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719783-T-A

77226620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719779-G-A

77226681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719723-T-C

77226684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719720-A-G

77226686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719718-A-G

77226686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719718-A-T

77226700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719704-A-G

77226838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719584-A-G

77227296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16719134-A-G

http://identifiers.org/hco/9/GRCh38#77227502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16718521-C-A

77227502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16718521-C-G

77227502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16718521-C-T

http://identifiers.org/hco/9/GRCh38#77227509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16718514-C-A

77227509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16718514-C-T

77227892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16718467-G-T

77227903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16718456-G-C

http://identifiers.org/hco/9/GRCh38#77228116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16718273-C-A

77228116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16718273-C-T

http://identifiers.org/hco/9/GRCh38#77228191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16718198-C-A

77228225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16718164-G-A

77228225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16718164-G-C

77228225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16718164-G-T

77228231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: stop gained
orthologous variants: 16718158-T-G

http://identifiers.org/hco/9/GRCh38#77228252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16718137-C-A

77228252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16718137-C-T

77228315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16716994-T-A

77228336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16716970-T-C

77228346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16716960-T-C

77237915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16712540-T-C

77238060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16712405-C-T

http://identifiers.org/hco/9/GRCh38#77238197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16712271-C-A

77238197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16712271-C-T

77238233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16712236-T-C

http://identifiers.org/hco/9/GRCh38#77238252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16712211-A-C

77238673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711857-C-G

77238701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711829-A-G

77238727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711804-C-T

77238744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711787-C-T

77239246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711346-G-C

77239393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711237-T-A

77239397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711233-A-T

77243519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16711027-T-C

77243606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16710956-T-C

77246953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16704253-A-G

77246987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16704188-C-T

77247162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703150-A-G

77247162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703150-A-T

77247177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703131-T-A

77247177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703131-T-C

http://identifiers.org/hco/9/GRCh38#77247181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16703127-A-C

77247181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703127-A-G

77247193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703115-T-C

77247194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703114-A-G

77247194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16703114-A-T

http://identifiers.org/hco/9/GRCh38#77247357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16702957-A-C

77247451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16702864-T-A

77249272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16701883-C-T

77249296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16701848-T-G

77251754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16700317-G-T

77252125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699975-T-G

77252126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699970-G-A

77252213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699893-A-G

77252213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699893-A-T

77252270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16699839-T-A

http://identifiers.org/hco/9/GRCh38#77252415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16699686-C-A

77252415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699686-C-G

77252564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699592-G-A

77252778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699377-T-C

77259360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699164-C-T

77259476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699052-C-T

77259477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16699051-G-A

77259555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16698427-A-G

77259774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16698241-T-G

77259993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16698039-T-A

77260280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16697632-A-G

77272652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16694025-G-A

77272787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16693906-G-T

77273249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16692520-G-T

77273388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16692387-A-G

77274015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16691432-T-G

http://identifiers.org/hco/9/GRCh38#77274088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16691359-A-C

77274605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16691176-G-A

77274664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16691103-A-G

77274685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16691082-C-T

77275248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688510-A-G

77275294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688471-A-G

77275294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688471-A-T

77275544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16688257-A-T

77275595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: synonymous variant
orthologous variants: 16688206-A-G

http://identifiers.org/hco/9/GRCh38#77275739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16688067-C-A

77275739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688067-C-T

http://identifiers.org/hco/9/GRCh38#77275789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16688031-C-A

77275789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688031-C-G

77275789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688031-C-T

http://identifiers.org/hco/9/GRCh38#77275804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16688030-C-A

77275804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16688030-C-G

77275951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687871-T-A

77275951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687871-T-G

77275975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687855-G-A

77275980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687850-C-T

77275991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687839-C-G

77275991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687839-C-T

77276077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16687777-T-G

77276296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687212-T-C

77276307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687201-A-G

77276307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16687201-A-T

77278597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16685392-T-G

77278783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16685211-G-T

77279707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16685094-C-G

77279915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16684942-A-T

http://identifiers.org/hco/9/GRCh38#77280039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16684851-C-A

77280077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16684834-A-G

77280137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16684787-A-G

77280222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16684705-C-T

77280388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16684563-A-G

77280388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16684563-A-T

77280394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16684558-T-C

77280573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16684382-T-C

77280724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16683821-C-T

77280813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16683749-T-G

77281815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16683355-A-T

77282205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16681963-T-A

http://identifiers.org/hco/9/GRCh38#77282223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16681945-C-A

77282223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16681945-C-G

77282223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16681945-C-T

77282330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16681845-A-G

77283144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16681364-T-G

77283479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16681042-A-G

77283717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680815-G-A

http://identifiers.org/hco/9/GRCh38#77283737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16680792-C-A

77283737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680792-C-G

77283739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680790-G-A

77283758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680774-A-T

77283982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680564-G-T

77284021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680533-A-T

77284026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16680528-A-T

77292242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16679591-C-T

77292967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16678952-G-A

77293068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16678860-C-T

77293392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16678599-A-G

77293427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16678564-G-A

77293527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16678464-T-A

77293527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16678464-T-C

77293646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16678376-A-G

77293646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16678376-A-T

77293758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16678284-A-G

http://identifiers.org/hco/9/GRCh38#77295469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16676545-C-A

77295469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16676545-C-T

77295530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16676487-G-A

77295561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16676455-A-G

77295768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16676248-T-A

77295768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16676248-T-C

77295768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16676248-T-G

77301656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16673477-G-A

77301672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16673457-T-C

77301683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16673444-A-G

77301692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16673437-T-C

77301894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16673284-G-A

77302843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16673035-T-A

77302875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16672997-T-C

77303084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16672798-T-C

77303084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16672798-T-G

77303140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16672751-A-G

77303209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16672688-T-G

77305428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16672040-T-A

77305518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16671948-T-A

77305518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16671948-T-C

77305518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16671948-T-G

77305586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 16671886-G-A

77305586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 16671886-G-T

77305602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 16671870-A-G

77305605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 16671867-T-C

77305737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16671741-C-T

77305757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16671721-G-T

77305870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16671613-T-C

http://identifiers.org/hco/9/GRCh38#77306196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16671352-A-C

77307668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16669739-G-A

77307819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16669614-A-G

77308041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16669163-A-G

77308068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16669136-G-A

77308084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16669123-C-T

77308125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16669083-C-G

77308125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16669083-C-T

77308134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16669074-T-C

77308255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16669012-A-G

77313552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16665879-T-C

77313740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16665670-A-G

http://identifiers.org/hco/9/GRCh38#77313925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16665498-C-A

77313930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16665493-G-T

77313938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16665485-A-G

77314006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665422-A-G

77314006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665422-A-T

77314024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665404-G-A

77314024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665404-G-T

77314033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665395-C-T

77314063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665365-A-G

77314063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16665365-A-T

77314212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16665200-A-G

77314346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16665083-T-C

77314378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664904-A-G

77314378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664904-A-T

http://identifiers.org/hco/9/GRCh38#77314513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16664597-C-A

77314513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16664597-C-T

77314657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16664453-A-G

http://identifiers.org/hco/9/GRCh38#77314728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16664387-C-A

77314728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664387-C-G

77314728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664387-C-T

77314766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664350-T-G

http://identifiers.org/hco/9/GRCh38#77314806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16664314-C-A

77314806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664314-C-T

77314902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664254-A-G

77315020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664215-G-A

77315134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664120-T-C

77315161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664092-T-A

77315180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664075-T-C

http://identifiers.org/hco/9/GRCh38#77315190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16664065-C-A

77315190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16664065-C-G

http://identifiers.org/hco/9/GRCh38#77315223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16664032-C-A

77315497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663764-A-G

77315528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663741-T-A

77315563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663707-T-A

77315563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663707-T-C

77315613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663658-T-C

77315635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663636-A-G

77315913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663203-A-T

77316024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663043-A-G

77316031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16663036-A-G

http://identifiers.org/hco/9/GRCh38#77316115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16662935-A-C

77316138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16662904-A-G

77316139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16662903-T-C

77316189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16662857-C-T

77316257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16662789-A-G

77316386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16662660-A-G

77316400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16662646-C-G

77316400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16662646-C-T

77316439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16662610-T-C

77316465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16662584-A-G

http://identifiers.org/hco/9/GRCh38#77317572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16660266-C-A

77317572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16660266-C-T

77317583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16660255-T-A

77317583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16660255-T-C

http://identifiers.org/hco/9/GRCh38#77317691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16660153-C-A

77317691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16660153-C-T

http://identifiers.org/hco/9/GRCh38#77318241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16659582-C-A

77318241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16659582-C-T

77318421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16659402-T-C

77318592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 16659231-G-A

77318607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16659216-C-T

77318746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16659100-A-T

77318777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16659068-A-G

http://identifiers.org/hco/9/GRCh38#77319509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16657563-C-A

77319509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16657563-C-T

http://identifiers.org/hco/9/GRCh38#77319517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16657555-C-A

77319517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16657555-C-G

77319581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16657464-T-C

http://identifiers.org/hco/9/GRCh38#77319810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16657287-C-A

77319810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16657287-C-T

77320329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16656707-C-G

77320331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16656705-A-G

http://identifiers.org/hco/9/GRCh38#77320474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16656522-A-C

77321042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16655885-G-A

77321042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16655885-G-T

77321047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16655880-A-G

77321114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16655822-A-T

77321133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16655803-A-G

77321333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16655601-A-G

77321491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 16655471-G-T

http://identifiers.org/hco/9/GRCh38#77321893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16654846-C-A

77321893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16654846-C-G

http://identifiers.org/hco/9/GRCh38#77321987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16654716-C-A

77322216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16654384-G-T

77322615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16654024-A-T

77322639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16654000-A-T

77322650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16653989-A-T

http://identifiers.org/hco/9/GRCh38#77322924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16653694-C-A

77322924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16653694-C-T

http://identifiers.org/hco/9/GRCh38#77323027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16653606-A-C

77323043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16653592-T-G

77323066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: splice acceptor variant
orthologous variants: 16653569-G-A

77323466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16653009-G-A

77323669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16652837-A-G

77323811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16652707-T-G

77323883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16652677-T-G

77323915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16652664-C-T

77323993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16652571-G-T

http://identifiers.org/hco/9/GRCh38#77324010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16652554-A-C

77324010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16652554-A-T

77330515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16646957-C-G

77330515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16646957-C-T

77331910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16646143-A-G

77332031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16646042-C-T

77332037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16646036-T-C

77332038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16646035-C-T

77332042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: synonymous variant
orthologous variants: 16646031-T-C

77332053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16646020-A-G

77332094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16645979-A-G

http://identifiers.org/hco/9/GRCh38#77332142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16645935-C-A

77332142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16645935-C-G

77332142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16645935-C-T

77332222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16645848-A-G

http://identifiers.org/hco/9/GRCh38#77332494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16645626-A-C

77334707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16645321-G-C

77334905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16644972-A-T

77335201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16644708-A-G

77337511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16643542-C-T

77337611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16643447-A-G

77337656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16643402-A-G

77337690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16642943-G-A

http://identifiers.org/hco/9/GRCh38#77337709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16642924-A-C

77337793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16642877-A-G

77337793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16642877-A-T

77337862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16642809-A-T

http://identifiers.org/hco/9/GRCh38#77339301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16642459-A-C

77339301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16642459-A-G

77339340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16642422-C-T

77339395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16642387-T-C

77339515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: splice acceptor variant
orthologous variants: 16642267-G-A

77339515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: splice acceptor variant
orthologous variants: 16642267-G-C

77339515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: splice acceptor variant
orthologous variants: 16642267-G-T

77339595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16642187-T-C

77339964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16641819-T-A

77339964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16641819-T-C

77340079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16641594-A-G

77340170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16641482-T-C

77340252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16641400-T-C

77340290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16641362-C-T

77340334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641321-A-G

77340461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16641203-C-T

77340575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640994-T-C

77340593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640977-T-C

77340595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640975-T-C

77340596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640974-C-G

77340596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640974-C-T

77340611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640959-T-A

http://identifiers.org/hco/9/GRCh38#77340625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16640945-A-C

77340625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640945-A-G

77340660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16640913-G-A

77340796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16640461-T-C

77340796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16640461-T-G

http://identifiers.org/hco/9/GRCh38#77341000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16640270-C-A

77341023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16640247-G-A

77341366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16639931-C-T

77344114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16638517-T-C

77344761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16638141-G-A

77344873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16638074-A-G

http://identifiers.org/hco/9/GRCh38#77344914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16638033-A-C

77345030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16637922-G-A

77345030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16637922-G-T

77345178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16637774-G-A

77345178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16637774-G-T

77345238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16637714-T-C

77345293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16637669-T-C

77345339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16637624-T-C

77345357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16637610-G-T

http://identifiers.org/hco/9/GRCh38#77351110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16636294-C-A

77351148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16636258-A-G

77351148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16636258-A-T

http://identifiers.org/hco/9/GRCh38#77351191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16636202-C-A

77351191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16636202-C-G

77351191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16636202-C-T

77351214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16636192-A-G

77352067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16635902-T-A

77352109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16635852-A-G

77352120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16635846-G-A

77352184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16635799-A-G

77352187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16635796-A-G

http://identifiers.org/hco/9/GRCh38#77353052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16633857-A-C

77353240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16633670-G-A

77353403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16633459-T-A

77353403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16633459-T-C

77353403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16633459-T-G

77353418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16633444-A-G

77353418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16633444-A-T

77356100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16633155-T-C

77356149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16633114-T-C

77356517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16632815-C-T

77356699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16632736-G-T

77357451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16632003-A-G

77357602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631944-T-G

http://identifiers.org/hco/9/GRCh38#77357644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16631900-C-A

77357644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631900-C-G

77357644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631900-C-T

77357904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631659-T-G

77358071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631490-T-C

77358077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631484-T-C

77358417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16631224-A-G

77358455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631187-A-T

http://identifiers.org/hco/9/GRCh38#77358482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16631163-C-A

77358487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631158-T-C

77358557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631099-A-G

http://identifiers.org/hco/9/GRCh38#77358563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16631093-C-A

77358563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631093-C-T

77358581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16631075-G-C

http://identifiers.org/hco/9/GRCh38#77358607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16631065-A-C

77358774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16630815-C-T

77359039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16630418-G-A

77359039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16630418-G-T

77359421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16630030-T-A

77359502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16629943-G-T

77359565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16629889-G-C

77359574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16629880-T-A

77359909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16629420-A-T

77360332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16629070-T-C

http://identifiers.org/hco/9/GRCh38#77360485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16628930-A-C

77360485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16628930-A-G

77360488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16628927-G-A

77360489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16628926-T-G

77364955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16625548-T-C

http://identifiers.org/hco/9/GRCh38#77365005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16625496-A-C

77365021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16625480-A-G

http://identifiers.org/hco/9/GRCh38#77365359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16625164-C-A

77365359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16625164-C-G

77365376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16625147-G-A

http://identifiers.org/hco/9/GRCh38#77365410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16625111-C-A

77365410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16625111-C-G

77365523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16625005-G-A

77365656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16624855-T-A

77365664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16624847-A-G

77365699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16624812-A-T

77365708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16624801-T-G

77365713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16624796-A-G

77366659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623426-T-A

77366659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623426-T-C

77366659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623426-T-G

77366844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: synonymous variant
orthologous variants: 16623239-C-T

77366885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623198-T-C

77366886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623197-T-C

77366911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623176-T-A

77366911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623176-T-C

77366922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623165-T-C

77367008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623087-G-A

77367008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623087-G-C

77367008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16623087-G-T

77367156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622937-G-A

77367159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622934-T-C

77367231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622862-C-T

77367248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622777-A-G

77367270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622747-A-G

77367305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622671-A-G

77367491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16622499-A-G

77367717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16621490-A-G

77368028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16621223-G-A

77368028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16621223-G-T

77368150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16621097-T-G

77368235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16620206-T-C

77368268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16620174-T-C

77368476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619968-T-A

77368490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619956-T-C

77368835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619709-A-G

77368938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619522-A-T

77368940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619520-C-T

77369176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619148-T-G

77369284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16619053-A-G

http://identifiers.org/hco/9/GRCh38#77369286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16619051-A-C

77369371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16618961-T-C

77369465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618843-G-A

77369491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618812-A-T

http://identifiers.org/hco/9/GRCh38#77369778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16618578-A-C

77369787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618569-T-C

77370232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618236-A-G

77370248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618230-G-A

77370248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618230-G-T

http://identifiers.org/hco/9/GRCh38#77370314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16618164-C-A

77370314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: synonymous variant
orthologous variants: 16618164-C-T

77370317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16618161-G-A

77370317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16618161-G-C

77370371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618113-A-T

http://identifiers.org/hco/9/GRCh38#77370389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16618095-C-A

77370389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618095-C-G

77370389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618095-C-T

77370390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618094-T-A

77370390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618094-T-C

77370390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618094-T-G

77370394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16618090-A-T

77370417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 16618060-G-A

77370429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16618048-G-A

77370513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16617964-G-A

77370552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16617925-A-G

77370614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16617864-A-T

77370622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16617856-T-C

http://identifiers.org/hco/9/GRCh38#77370671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16617813-C-A

77370671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16617813-C-T

77370784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16617711-A-G

77371046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: missense variant
orthologous variants: 16617455-G-A

77371184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16617319-T-C

77381832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613914-T-C

77381832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613914-T-G

77381857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613890-T-C

77381860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613887-A-G

77381884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613859-G-C

77381916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613306-T-C

77381920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613301-T-C

77382101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613117-T-C

77382116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16613102-G-T

77382327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612905-A-G

77382327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612905-A-T

http://identifiers.org/hco/9/GRCh38#77382334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16612898-C-A

77382334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612898-C-T

77382371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612860-A-G

77382438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612806-G-C

77382438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612806-G-T

77382452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612792-T-A

77382453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612791-A-G

77382453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612791-A-T

77382541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612707-T-G

77382561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612682-G-T

77382684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612548-T-C

77382922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16612361-A-T

77383419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16611893-G-A

77383639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16611646-T-C

77384155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610924-A-G

77384157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610922-G-T

77384169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610910-T-A

77384201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610873-T-C

77384291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610791-T-C

77384440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610653-A-G

http://identifiers.org/hco/9/GRCh38#77384457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16610636-C-A

77384457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610636-C-T

http://identifiers.org/hco/9/GRCh38#77384490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16610609-C-A

77384490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610609-C-T

77384491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610608-A-G

77384509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16610591-A-G

77384602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 16610507-G-A

77384602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, missense_variant
orthologous variants: 16610507-G-T

77384669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, missense_variant
orthologous variants: 16610440-G-C

77384669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, missense_variant
orthologous variants: 16610440-G-T

77384777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16610344-A-G

77385073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16610042-T-A

77385073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16610042-T-C

77385294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609829-A-G

77385378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609760-T-A

77385384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609755-A-G

77385676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609449-T-G

77385863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609225-A-T

77385916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609190-A-T

77386037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609122-A-G

77386114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609094-T-G

77386134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16609074-A-G

77387437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16607325-A-G

77388301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16606415-A-G

77388301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16606415-A-T

77389680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16605986-T-A

http://identifiers.org/hco/9/GRCh38#77389708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16605955-C-A

77389708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron variant
orthologous variants: 16605955-C-G

77389964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16605713-T-C

77390257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16605414-T-C

77390854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16605087-T-C

77391088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604787-T-C

77391089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604786-A-G

77391332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604586-T-A

77391731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604277-C-T

77391819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604177-C-T

77391823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604173-C-T

77392101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16603871-T-C

77392148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16603835-G-C

77392162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16603830-G-C

77392415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602440-T-C

77392472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602385-A-G

77395667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602299-G-A

77395949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602075-A-G

77396169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601871-T-G

77396193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601847-A-G

77396211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601829-G-T

77397981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16600734-C-T

77398774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16600036-T-G

77399762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16599547-G-T

77402105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16599041-C-T

77402851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598408-G-A

77402851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598408-G-T

77403110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598188-A-G

77405744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596991-G-T

http://identifiers.org/hco/9/GRCh38#77405753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16596982-C-A

77405753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596982-C-G

77405753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596982-C-T

77405809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596914-G-A

77405809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596914-G-T

77406031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596693-T-C

http://identifiers.org/hco/9/GRCh38#77406033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16596691-A-C

77406033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596691-A-G

77406033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596691-A-T

77406034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596690-T-C

77406040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596684-G-A

77406040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596684-G-T

77406081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596657-T-C

http://identifiers.org/hco/9/GRCh38#77406097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16596641-C-A

77406109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596629-T-A

77407467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596595-G-T

77407511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596552-A-T

77407662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596396-A-G

77407668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596390-A-T

77407680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596377-T-C

http://identifiers.org/hco/9/GRCh38#77407779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16596303-C-A

77407779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596303-C-G

77407841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596251-C-G

77407841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16596251-C-T

77408163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16595802-T-C

http://identifiers.org/hco/9/GRCh38#77408177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16595788-A-C

77414870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16595623-C-T

77415121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16595408-G-C

77415834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16594389-T-C

http://identifiers.org/hco/9/GRCh38#77416028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16594202-A-C

http://identifiers.org/hco/9/GRCh38#77416032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16594198-A-C

77416032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16594198-A-G

77416042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16594188-G-C

77416042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16594188-G-T

77416120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16594116-G-A

http://identifiers.org/hco/9/GRCh38#77416226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16594054-C-A

77416226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16594054-C-G

77416226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16594054-C-T

http://identifiers.org/hco/9/GRCh38#77416314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16593982-C-A

http://identifiers.org/hco/9/GRCh38#77416315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16593981-A-C

77416344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593952-G-A

http://identifiers.org/hco/9/GRCh38#77416354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16593942-C-A

77416410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593894-T-C

77416430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593874-A-T

77416708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593601-C-T

77416731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593578-T-C

http://identifiers.org/hco/9/GRCh38#77416819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16593500-C-A

77416819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593500-C-G

77417072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16593243-A-G

http://identifiers.org/hco/9/GRCh38#77417536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16592817-C-A

77417536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16592817-C-T

77417559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16592800-G-A

77417559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16592800-G-T

77417624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16592724-G-A

77417642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 16592707-G-C

http://identifiers.org/hco/9/GRCh38#77417661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16592690-C-A

77417754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592620-G-T

77417782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592604-G-T

77417794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 16592596-G-C

77417794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 16592596-G-T

77417826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592567-G-A

77417826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592567-G-C

77417826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592567-G-T

77417839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592555-A-G

77417855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592538-C-T

77417947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592458-C-T

77418826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16592046-A-G

77418967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591933-T-G

http://identifiers.org/hco/9/GRCh38#77418981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16591919-A-C

77418981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591919-A-G

77419120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591800-G-T

77419145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591779-A-T

77419207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591725-T-C

http://identifiers.org/hco/9/GRCh38#77419246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16591690-C-A

77419263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591673-A-T

77419305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591631-A-G

77419443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591512-A-G

77419454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591501-G-A

77419454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591501-G-T

77419473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591482-A-G

77419630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591348-C-G

77419684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591295-G-A

77419740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591255-C-T

77419891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591151-G-A

77419891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591151-G-T

77420024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16591020-A-G

http://identifiers.org/hco/9/GRCh38#77420285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16590799-C-A

http://identifiers.org/hco/9/GRCh38#77420838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16590276-C-A

77420838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16590276-C-T

77420918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16590195-C-T

77421133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16589938-T-A

77421242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16589834-T-C

77421455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16589636-T-A

http://identifiers.org/hco/9/GRCh38#77421500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#16589591-C-A

77421500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1908
most severe consequence: 3 prime UTR variant
orthologous variants: 16589591-C-T