http://identifiers.org/hco/7/GRCh38#92246004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#3853079-C-A

92246004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3853079-C-T

http://identifiers.org/hco/7/GRCh38#92246048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#3853035-C-A

92246048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3853035-C-T

92246064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 3853020-G-C

92246064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 3853020-G-T

92246110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 3852974-A-G

http://identifiers.org/hco/7/GRCh38#92246355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#3852733-C-A

92246399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5 prime UTR variant
orthologous variants: 3852724-G-A

92246399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 5 prime UTR variant
orthologous variants: 3852724-G-T

92246565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron_variant, undefined
orthologous variants: 3852549-C-T

http://identifiers.org/hco/7/GRCh38#92246667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3852488-C-A

92246667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3852488-C-G

92246667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3852488-C-T

http://identifiers.org/hco/7/GRCh38#92246831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3852303-C-A

92248203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3851270-A-G

92248215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3851258-T-A

92248278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3851194-A-G

92248846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3850719-C-T

92250662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3850570-G-A

92250745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3850490-G-C

92250749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3850486-G-A

92250970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3850275-T-C

92251516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3849722-T-C

92251560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3849682-C-T

92251921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3849450-A-G

92256024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3845123-A-G

92256024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3845123-A-T

92256251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3845037-G-A

92256591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3844788-G-A

92257244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3844318-A-G

92257437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3844109-T-C

92257490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3844077-T-C

92258207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3843697-C-G

92259440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3841896-A-G

92259511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3841837-G-T

92259737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3841666-C-T

92259922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3841496-A-G

http://identifiers.org/hco/7/GRCh38#92260101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3841314-C-A

92260182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3841245-C-T

92260223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3841213-T-C

92261489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3840625-T-G

92261654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3840461-A-G

92261736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3840382-G-A

92262071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3840079-A-G

92262072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3840078-A-G

http://identifiers.org/hco/7/GRCh38#92262101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3840050-A-C

92263052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3839782-A-G

92263145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3839681-A-G

http://identifiers.org/hco/7/GRCh38#92268245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3838738-A-C

92280413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3836733-T-A

92280413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3836733-T-G

92280416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3836730-A-G

92280416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3836730-A-T

92281502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3835727-G-A

92281520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3835709-G-T

92283155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3834819-A-G

92292098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3828737-G-T

92292150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3828685-A-G

92292150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3828685-A-T

92293151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3825981-C-G

92293642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3825574-A-G

92293647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3825569-T-C

92294681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3823128-G-T

92294831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3822846-T-C

http://identifiers.org/hco/7/GRCh38#92295003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3822678-C-A

http://identifiers.org/hco/7/GRCh38#92295123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3822558-C-A

92295123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: missense variant
orthologous variants: 3822558-C-T

http://identifiers.org/hco/7/GRCh38#92295129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3822552-C-A

92295129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: missense variant
orthologous variants: 3822552-C-T

92295234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3822479-A-G

92307588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 3819495-G-A

92308313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3819175-C-T

92308351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3819146-A-T

http://identifiers.org/hco/7/GRCh38#92310333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3818077-C-A

92310333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3818077-C-T

92312335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3808960-A-G

92312827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3808384-A-G

92313220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3807985-A-G

92313271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3807929-C-G

92314313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3807461-A-G

92314318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3807456-A-T

92319108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3806048-C-T

92319208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3805886-T-A

92319208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3805886-T-C

http://identifiers.org/hco/7/GRCh38#92319330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3805774-C-A

92319330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 3805774-C-T

92319514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 3805590-T-C

92319619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 3805519-G-T

92319639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3805501-T-A

92319639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3805501-T-C

http://identifiers.org/hco/7/GRCh38#92319643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3805488-C-A

92319656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3805476-T-A

92319656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3805476-T-C

http://identifiers.org/hco/7/GRCh38#92319660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3805472-A-C

92319660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3805472-A-G

92321715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3805186-T-G

92321889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3805019-C-T

92322210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3804766-G-A

92325904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3800895-T-C

http://identifiers.org/hco/7/GRCh38#92325996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3800818-A-C

92325996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3800818-A-G

http://identifiers.org/hco/7/GRCh38#92326033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3800781-C-A

92326033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3800781-C-T

92327144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3797399-A-G

92327144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3797399-A-T

92327191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3797351-A-G

92328984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3796354-T-G

92329012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3796321-G-T

92329107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3796238-A-G

92329484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3795769-C-T

92330122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3795170-C-G

92330410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3794744-T-C

92331080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3793801-G-A

92331080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3793801-G-T

92331857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3792967-C-G

92332203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3792686-T-C

92332224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3792665-G-T

92332245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3792644-C-T

92332461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3792451-C-T

http://identifiers.org/hco/7/GRCh38#92332534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3792399-C-A

92332534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3792399-C-T

92332736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3791326-C-T

http://identifiers.org/hco/7/GRCh38#92332926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3791143-A-C

92332997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3791072-G-A

92332997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3791072-G-C

92333481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3790570-G-C

92333949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3789770-C-T

http://identifiers.org/hco/7/GRCh38#92334221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3789534-A-C

92334325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3789455-T-C

92334455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3789343-A-G

http://identifiers.org/hco/7/GRCh38#92334523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3789286-A-C

92336913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3788109-G-T

92337442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3785854-T-C

92337546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3785747-G-T

92337617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3785686-A-G

92342804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3784387-G-A

92343089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 3784117-G-A

http://identifiers.org/hco/7/GRCh38#92343116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3784090-A-C

92343116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 3784090-A-T

92343277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3783941-T-A

92343277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3783941-T-C

92343282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3783936-T-A

92343811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3783571-A-G

92343948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3783438-T-C

http://identifiers.org/hco/7/GRCh38#92344507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3782993-A-C

92344857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782736-A-G

92344857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782736-A-T

92345123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782479-A-G

92345157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782449-A-G

92345209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782401-G-A

92345209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782401-G-C

92345209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3782401-G-T

http://identifiers.org/hco/7/GRCh38#92345312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3782353-C-A

92345877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3781819-A-T

92347135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3780560-A-G

92347142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3780553-C-G

92347147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3780548-C-G

92351186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3779596-G-T

92351624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3779255-G-A

92351638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3779241-A-G

92352188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3777900-T-C

92353098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3777044-A-G

92353110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3777032-A-T

92354333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3775735-A-G

92354521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3775570-A-G

92354607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3775484-T-G

92354614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3775477-T-C

92358282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3774361-C-T

92358395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3774262-G-A

92358656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3774023-C-T

92358685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3773998-A-G

92362353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3772469-T-A

92362419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3772424-A-G

92362639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3772242-C-G

92362687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3772197-C-G

92362922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3771440-T-C

92363506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3771227-G-A

92365464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3770315-T-A

92365464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3770315-T-C

92365498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3770279-G-A

92365572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3770215-G-T

92367063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3767477-T-A

92367063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3767477-T-C

92367250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3767261-A-G

92367794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3766609-A-T

92368204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3766470-A-G

92368773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3766218-C-G

92369160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3765858-G-A

92369282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3765764-G-C

92369452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3765599-T-C

92369652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3765452-A-G

92369688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3765420-T-G

92370096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3764875-G-A

92370195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3764782-G-C

92371186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763872-T-A

92371213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763845-G-C

92371213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763845-G-T

92371402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763301-G-A

92371402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763301-G-T

92371445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763265-T-C

92371448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: intron variant
orthologous variants: 3763262-T-G

92371634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3763080-G-T

92372948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3762676-T-A

92372948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3762676-T-C

92372948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3762676-T-G

92373057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3762566-C-T

92373418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3762217-A-G

http://identifiers.org/hco/7/GRCh38#92373542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3762094-C-A

92373612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3761868-T-C

92373674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3761799-A-G

92373711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3761766-A-G

92373711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3761766-A-T

92386590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 3756240-C-G

92386590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 3756240-C-T

92386677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756174-T-C

92386677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756174-T-G

92386695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756155-T-A

92386695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756155-T-C

92386695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756155-T-G

http://identifiers.org/hco/7/GRCh38#92386719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3756140-C-A

92386719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756140-C-G

92386719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756140-C-T

92386721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756138-A-G

92386724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756135-T-A

92386724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3756135-T-C

92386849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3755994-T-C

92387671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754989-A-T

92387689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754971-G-C

92387689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754971-G-T

92387714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754946-A-T

http://identifiers.org/hco/7/GRCh38#92387742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3754924-C-A

92388177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754362-G-A

92388177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754362-G-T

92388229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754334-G-A

92388244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754322-C-T

92388444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754169-G-C

92388584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754069-A-G

92388585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754068-A-G

92388632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3754024-C-T

92388912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3753761-A-G

92388912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3753761-A-T

92389180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3753534-C-T

92389259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3753426-G-A

92389566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3753151-A-G

92390341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3752728-T-C

92390758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3752380-A-G

92390790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3752348-A-G

http://identifiers.org/hco/7/GRCh38#92391032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3752105-A-C

92391099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3752043-G-T

http://identifiers.org/hco/7/GRCh38#92391133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3752012-C-A

92391133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3752012-C-T

92391205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 3751942-G-T

92391347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751800-A-G

http://identifiers.org/hco/7/GRCh38#92391361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3751788-C-A

92391361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751788-C-G

92391397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751752-G-T

92391410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751739-T-C

http://identifiers.org/hco/7/GRCh38#92391415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3751734-C-A

http://identifiers.org/hco/7/GRCh38#92391432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3751717-C-A

92391432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751717-C-G

92391541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751633-G-T

92391599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751574-C-T

http://identifiers.org/hco/7/GRCh38#92391642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3751536-A-C

92391955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3751235-A-G

92392132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3750514-G-A

92392132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3750514-G-T

http://identifiers.org/hco/7/GRCh38#92392133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3750513-C-A

92392133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3750513-C-T

92392399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3750262-G-A

92392403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3750258-C-G

92392782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3749904-C-G

92392879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3749657-G-A

http://identifiers.org/hco/7/GRCh38#92393057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3749499-A-C

92394439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3746639-A-G

92394692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3746229-G-A

92395205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3745573-A-T

92395259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3745517-T-G

92396169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3745092-T-C

92396328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3744928-A-G

http://identifiers.org/hco/7/GRCh38#92396443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3744810-C-A

92396443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3744810-C-G

92396573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3744682-T-C

http://identifiers.org/hco/7/GRCh38#92396583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3744672-A-C

92396583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3744672-A-G

http://identifiers.org/hco/7/GRCh38#92397480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3744099-C-A

92397480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3744099-C-T

92397568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3744036-A-G

92397570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3744034-G-A

92397734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3743892-G-A

92397734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3743892-G-T

http://identifiers.org/hco/7/GRCh38#92397833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743796-C-A

92397833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3743796-C-G

92397833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3743796-C-T

http://identifiers.org/hco/7/GRCh38#92397869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743760-C-A

92397871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743758-G-T

92397884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743742-G-A

92397884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743742-G-T

92397892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743735-T-A

92397892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743735-T-C

92397894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743733-T-C

92397999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743643-G-A

92397999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743643-G-T

http://identifiers.org/hco/7/GRCh38#92398068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743604-A-C

92398088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743584-A-G

http://identifiers.org/hco/7/GRCh38#92398138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743568-A-C

92398138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743568-A-G

http://identifiers.org/hco/7/GRCh38#92398163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743543-A-C

92398163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743543-A-G

92398166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743540-T-A

92398166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743540-T-C

http://identifiers.org/hco/7/GRCh38#92398196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743510-C-A

92398196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3743510-C-T

http://identifiers.org/hco/7/GRCh38#92398324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743382-A-C

92398345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 3743361-G-C

92398390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 3743316-A-G

http://identifiers.org/hco/7/GRCh38#92398496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3743210-A-C

92398623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 3743083-C-T

92398961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742742-C-G

92398961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742742-C-T

92399003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742702-G-A

92399003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742702-G-C

92399003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742702-G-T

92399224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742502-A-G

92399233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742493-T-C

http://identifiers.org/hco/7/GRCh38#92399236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3742490-A-C

92399236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742490-A-G

92399262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742466-T-C

92399265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742463-G-T

92399267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742461-T-C

92399273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742455-A-G

http://identifiers.org/hco/7/GRCh38#92399310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3742418-C-A

92399310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3742418-C-T

92399633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3 prime UTR variant
orthologous variants: 3742090-G-A

92399633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3 prime UTR variant
orthologous variants: 3742090-G-T

http://identifiers.org/hco/7/GRCh38#92400333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22215
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#3741403-C-A