136250079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130345-G-T

136250084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130351-G-A

136250144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130405-G-T

136250167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130429-G-A

136250167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130429-G-T

136250217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130478-G-A

136250217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130478-G-C

136250217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130478-G-T

136250270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130531-C-G

136250270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130531-C-T

136250300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130561-G-A

136250349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130614-G-T

136250352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130617-G-A

136250409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130685-G-A

136250480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130761-C-G

136250480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26130761-C-T

136250540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130819-T-A

136250540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130819-T-C

136250584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130873-A-G

136250612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130899-A-G

http://identifiers.org/hco/9/GRCh38#136250700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26130980-C-A

136250700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26130980-C-T

136250739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131009-G-C

http://identifiers.org/hco/9/GRCh38#136250783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26131047-C-A

136250961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131197-C-G

136251000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131228-G-A

136251086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131310-T-C

http://identifiers.org/hco/9/GRCh38#136251098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26131320-C-A

136251098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131320-C-T

136251122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131344-A-T

http://identifiers.org/hco/9/GRCh38#136251135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26131356-C-A

136251135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131356-C-T

136251144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26131365-C-T

http://identifiers.org/hco/9/GRCh38#136252647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26136288-C-A

136252759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136398-G-T

136252813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136452-C-G

136252813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136452-C-T

136252819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136458-G-C

136252819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136458-G-T

136252827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136466-G-T

http://identifiers.org/hco/9/GRCh38#136252833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26136472-C-A

136252833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136472-C-T

136252880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136540-G-A

136252880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136540-G-C

136252880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136540-G-T

136252925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136585-G-A

136252925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136585-G-C

136252925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136585-G-T

136252964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136624-G-T

http://identifiers.org/hco/9/GRCh38#136252966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26136626-C-A

136252966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136626-C-T

136252997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136657-T-C

136253001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136661-G-A

136253001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136661-G-T

http://identifiers.org/hco/9/GRCh38#136253214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26136737-C-A

136253214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136737-C-T

136253398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136827-G-C

136253449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136878-A-G

136253449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3 prime UTR variant
orthologous variants: 26136878-A-T

http://identifiers.org/hco/9/GRCh38#136253615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26136960-C-A

136253615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26136960-C-T

136253640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26136985-G-A

136253640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26136985-G-T

http://identifiers.org/hco/9/GRCh38#136253714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26137086-C-A

136253714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137086-C-T

136253747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137119-G-A

136253920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137292-T-C

http://identifiers.org/hco/9/GRCh38#136254051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26137366-C-A

136254051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137366-C-T

136254241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137568-G-A

136254241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137568-G-T

136254260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137587-C-T

136254279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137606-C-T

136254314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137641-T-C

136254314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137641-T-G

136254374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137653-G-A

136254374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137653-G-C

136254431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137662-G-A

136254431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137662-G-T

136254440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137671-G-A

136254440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137671-G-T

136254443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26137674-G-A

136254684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26137915-A-G

http://identifiers.org/hco/9/GRCh38#136254694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26137925-C-A

136254694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, undefined
orthologous variants: 26137925-C-G

136254694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, undefined
orthologous variants: 26137925-C-T

136254885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26138119-G-T

http://identifiers.org/hco/9/GRCh38#136255057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26138288-A-C

136255057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26138288-A-G

136255224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26138469-G-A

136255224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26138469-G-C

136255224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26138469-G-T

http://identifiers.org/hco/9/GRCh38#136255229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26138477-A-C

http://identifiers.org/hco/9/GRCh38#136255234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26138482-C-A

136255270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26138516-G-A

136255270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26138516-G-T

136255311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26138556-C-G

136255318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26138563-C-T

http://identifiers.org/hco/9/GRCh38#136255525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26138698-C-A

136255664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26138850-G-T

136255698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26138884-G-T

136255699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26138885-A-G

136255724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26138910-G-A

136255724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26138910-G-T

http://identifiers.org/hco/9/GRCh38#136255726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26138912-C-A

136255731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 26138917-G-A

136255731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 26138917-G-T

http://identifiers.org/hco/9/GRCh38#136255747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#26138940-C-A

136255747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26138940-C-T

http://identifiers.org/hco/9/GRCh38#136255883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26139059-C-A

136255884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26139060-T-C

136255942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26139147-G-C

136256085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26139284-T-A

136256085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26139284-T-C

136256145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26139301-G-A

136256145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26139301-G-T

136256374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26139495-G-A

136256374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26139495-G-T

136256375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26139496-T-C

136256412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, undefined
orthologous variants: 26139533-A-G

136256600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139694-G-T

136256639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139751-C-T

http://identifiers.org/hco/9/GRCh38#136256644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26139756-C-A

136256644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139756-C-T

136256648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139760-A-G

136256659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139771-G-A

136256794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26139904-C-T

http://identifiers.org/hco/9/GRCh38#136256825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26139938-C-A

136256854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139967-G-A

136256854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139967-G-T

136256869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26139986-G-C

136256898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26140015-G-A

http://identifiers.org/hco/9/GRCh38#136256903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26140020-C-A

136256903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26140020-C-T

136256947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26140045-G-T

136257469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26140352-G-A

136257698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26140555-G-T

136257725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26140580-G-A

136258226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141007-C-T

136258390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141189-C-G

136258494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141256-G-A

136258552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141314-C-T

http://identifiers.org/hco/9/GRCh38#136258580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141343-A-C

136258580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141343-A-T

136258586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141349-A-G

136258587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141350-A-G

136258713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26141476-C-T

http://identifiers.org/hco/9/GRCh38#136258911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141698-C-A

136258911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26141698-C-G

136258911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant
orthologous variants: 26141698-C-T

136258924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 26141711-G-A

136258924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 26141711-G-T

136258979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26141769-A-G

http://identifiers.org/hco/9/GRCh38#136258986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141773-C-A

http://identifiers.org/hco/9/GRCh38#136258996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141783-C-A

136259000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 26141787-G-T

136259022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141810-G-A

136259022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141810-G-T

http://identifiers.org/hco/9/GRCh38#136259024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141812-A-C

136259024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141812-A-G

http://identifiers.org/hco/9/GRCh38#136259061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141821-C-A

136259061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141821-C-T

http://identifiers.org/hco/9/GRCh38#136259066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141826-A-C

136259066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141826-A-T

http://identifiers.org/hco/9/GRCh38#136259072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26141832-C-A

136259072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141832-C-T

136259108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141866-G-A

136259108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141866-G-T

136259308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26141956-G-A

136259395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26142045-G-C

136259395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26142045-G-T

136259403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26142053-A-G

136259510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142783-G-A

136259510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142783-G-C

136259510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142783-G-T

136259576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142838-G-T

136259577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142839-G-A

136259577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142839-G-T

136259595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142871-G-A

136259595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26142871-G-T

136259758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143015-G-A

136259914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143169-G-T

136259918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143173-C-T

136259921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143176-C-T

136260021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143256-G-C

136260021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143256-G-T

136260037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143272-G-T

136260042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143277-A-G

http://identifiers.org/hco/9/GRCh38#136260065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26143302-C-A

136260077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143314-G-A

136260077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143314-G-T

136260080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26143317-T-C

http://identifiers.org/hco/9/GRCh38#136260136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26143366-C-A

136260136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26143366-C-T

136260169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26143399-G-A

136260169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26143399-G-T

http://identifiers.org/hco/9/GRCh38#136260190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26143420-C-A

136260190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26143420-C-T

http://identifiers.org/hco/9/GRCh38#136260216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26143446-A-C

136260216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26143446-A-G

136260246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26143476-C-G

136260246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26143476-C-T

136261802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144102-G-T

136261883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144186-C-T

136261908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144223-C-T

136262108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144357-G-A

136262120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144369-G-C

136262135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144384-C-G

136262135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144384-C-T

136262160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144409-G-A

136262161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144410-C-T

http://identifiers.org/hco/9/GRCh38#136262234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26144473-C-A

136262234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144473-C-T

136262235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144474-G-A

136262235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144474-G-C

136262235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144474-G-T

http://identifiers.org/hco/9/GRCh38#136262251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26144726-C-A

136262258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144733-G-A

136262258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144733-G-T

http://identifiers.org/hco/9/GRCh38#136262270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26144745-C-A

136262270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144745-C-T

136262367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26144823-G-A

136262367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26144823-G-T

http://identifiers.org/hco/9/GRCh38#136262418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26144853-C-A

136262418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26144853-C-T

136262492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144932-A-G

http://identifiers.org/hco/9/GRCh38#136262497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26144937-C-A

136262497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144937-C-T

http://identifiers.org/hco/9/GRCh38#136262515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26144975-C-A

136262515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26144975-C-T

136262579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26145043-G-A

136262579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26145043-G-T

http://identifiers.org/hco/9/GRCh38#136262603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26145070-C-A

136262603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26145070-C-T

136262842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26145295-C-T

http://identifiers.org/hco/9/GRCh38#136263265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26145668-C-A

136263468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26145793-T-C

136263634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: synonymous variant
orthologous variants: 26145889-G-T

136263638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26145893-T-A

136263638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26145893-T-C

136263638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense variant
orthologous variants: 26145893-T-G

136263848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26146061-G-A

136263848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26146061-G-T

136263893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26146082-G-A

136263893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26146082-G-T

http://identifiers.org/hco/9/GRCh38#136263899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146088-A-C

136263899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26146088-A-G

http://identifiers.org/hco/9/GRCh38#136263926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146115-A-C

136263926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146115-A-G

136263929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146118-G-T

136263954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146139-G-A

136263954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146139-G-T

136263976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146156-T-A

136263976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146156-T-C

136263978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146158-G-T

http://identifiers.org/hco/9/GRCh38#136263990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146170-C-A

136263990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146170-C-T

136264006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146186-G-A

136264056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146242-G-T

http://identifiers.org/hco/9/GRCh38#136264083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146264-C-A

136264083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146264-C-G

136264083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146264-C-T

136264106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146283-G-A

136264106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146283-G-T

http://identifiers.org/hco/9/GRCh38#136264112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146289-C-A

136264112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146289-C-T

136265640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146400-A-G

http://identifiers.org/hco/9/GRCh38#136265660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146420-C-A

136265698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146461-C-T

136265714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146477-G-A

136265714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146477-G-C

136265820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146520-T-A

136265820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146520-T-C

136265904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146599-A-T

http://identifiers.org/hco/9/GRCh38#136265905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146600-C-A

136265905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146600-C-G

136265905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146600-C-T

136265912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26146604-T-C

136266074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26146750-G-T

136266202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26146866-G-A

136266202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26146866-G-C

http://identifiers.org/hco/9/GRCh38#136266236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146885-C-A

136266236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26146885-C-T

http://identifiers.org/hco/9/GRCh38#136266244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146893-C-A

136266244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26146893-C-T

http://identifiers.org/hco/9/GRCh38#136266319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26146959-C-A

136266319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26146959-C-T

136266404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147010-A-G

136266430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147029-A-G

136266430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147029-A-T

http://identifiers.org/hco/9/GRCh38#136266432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26147031-C-A

136266432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147031-C-G

136266432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147031-C-T

136266507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26147108-C-T

http://identifiers.org/hco/9/GRCh38#136266555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26147155-C-A

136266607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147199-G-A

136266607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147199-G-T

136267159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147342-G-A

136267159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147342-G-T

136267196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147380-A-G

136267196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26147380-A-T

http://identifiers.org/hco/9/GRCh38#136267220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26147404-A-C

http://identifiers.org/hco/9/GRCh38#136267239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26147422-C-A

136267239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147422-C-T

136267264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147431-C-T

136267290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147449-A-G

136267378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147513-G-A

136267458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26147593-C-T

http://identifiers.org/hco/9/GRCh38#136267494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26147629-C-A

136267494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26147629-C-G

136267499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26147634-T-C

136267548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147683-G-T

136267572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147704-G-A

136267572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147704-G-C

136267572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147704-G-T

136267580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147717-A-G

136267621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147778-C-T

136267624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147781-G-A

136267655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147820-G-A

136267655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147820-G-T

136267700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147866-G-A

136267807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26147971-G-A

136267858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148022-C-G

136267858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148022-C-T

136267907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148070-G-T

136267989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148127-T-G

http://identifiers.org/hco/9/GRCh38#136268067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26148189-C-A

136268067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26148189-C-G

136268067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26148189-C-T

136268145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148269-G-C

136268145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148269-G-T

136268159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148283-G-A

136268159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148283-G-T

136268160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148284-G-C

136268160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148284-G-T

136268171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148292-G-T

136268172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148293-C-T

136268181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148302-A-G

136268185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148320-G-A

136268185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148320-G-T

136268197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148332-G-A

http://identifiers.org/hco/9/GRCh38#136268203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26148338-C-A

136268203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148338-C-T

136268234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148359-A-G

136268274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148388-G-A

136268274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148388-G-T

136268450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148531-G-C

136268762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26148788-T-C

136269484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26149424-C-T

136274694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26155091-T-C

136274694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26155091-T-G

136274711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26155108-G-A

136274737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26155134-A-G

136274755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26155152-G-T

136274974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26155365-G-A

136274974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26155365-G-T

136275003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 26155394-A-G

http://identifiers.org/hco/9/GRCh38#136276220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26156645-C-A

136276232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 26156657-G-A

136276386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26156808-T-C

136276549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26156917-G-T

http://identifiers.org/hco/9/GRCh38#136276654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26157027-C-A

136276654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26157027-C-T

http://identifiers.org/hco/9/GRCh38#136276767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26157157-C-A

136276767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26157157-C-T

136277008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26157338-A-G

136277120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26157436-G-A

http://identifiers.org/hco/9/GRCh38#136277294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#106538992-A-C

136277294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106538992-A-T

136279395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26159313-A-T

136279624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26159522-G-A

136279647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26159547-G-A

136280958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161261-T-C

136280996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161298-G-A

136280996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161298-G-T

136281059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161363-G-A

136281059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161363-G-T

http://identifiers.org/hco/9/GRCh38#136281103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26161404-C-A

136281103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161404-C-T

136281141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161440-C-T

http://identifiers.org/hco/9/GRCh38#136281142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26161441-A-C

136281175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26161478-C-T

136281594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26161881-G-A

136281594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26161881-G-C

136281594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26161881-G-T

136281653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26161940-C-T

http://identifiers.org/hco/9/GRCh38#136281706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26161994-A-C

136281706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26161994-A-G

136281721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162007-G-A

136281721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162007-G-T

http://identifiers.org/hco/9/GRCh38#136281751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26162030-C-A

136281977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162198-C-T

136281978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162199-G-A

136281978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162199-G-C

136281978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162199-G-T

http://identifiers.org/hco/9/GRCh38#136282141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26162362-A-C

136282393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162598-G-A

136282605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162762-G-A

136282735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26162851-G-A

http://identifiers.org/hco/9/GRCh38#136282763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26162876-A-C

136283718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26163628-G-A

136283943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26163819-G-A

http://identifiers.org/hco/9/GRCh38#136284009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26163842-C-A

136284015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26163850-C-G

http://identifiers.org/hco/9/GRCh38#136284021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26163856-C-A

http://identifiers.org/hco/9/GRCh38#136285804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26165729-C-A

136285815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26165736-A-G

136285824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26165745-G-A

136285824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26165745-G-T

http://identifiers.org/hco/9/GRCh38#136285844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26165761-C-A

136285844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26165761-C-T

136285854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26165771-G-A

136285858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26165775-C-T

136286088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 26165922-G-A

136286088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26165922-G-T

136286120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26165954-A-G

http://identifiers.org/hco/9/GRCh38#136286147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26165978-C-A

136286147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26165978-C-T

136286208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166039-T-C

136286226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166057-G-A

136286228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166059-G-A

136286228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166059-G-C

136286228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166059-G-T

136286256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166087-C-G

136286293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166109-G-A

136286293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166109-G-T

136286360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166176-G-A

136286360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166176-G-T

http://identifiers.org/hco/9/GRCh38#136286368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166184-C-A

136286368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166184-C-T

136286374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166191-G-A

136286374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166191-G-T

136286449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166265-C-T

136286478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166294-A-G

http://identifiers.org/hco/9/GRCh38#136286490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166306-C-A

http://identifiers.org/hco/9/GRCh38#136286576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166385-C-A

136286598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26166407-G-A

136286598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166407-G-T

http://identifiers.org/hco/9/GRCh38#136286610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166419-C-A

136286610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166419-C-G

136286610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166419-C-T

http://identifiers.org/hco/9/GRCh38#136286630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166441-C-A

136286630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166441-C-G

136286630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166441-C-T

136286660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166463-G-A

136286660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166463-G-T

136286688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26166491-G-T

http://identifiers.org/hco/9/GRCh38#136286717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166519-C-A

136286717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26166519-C-T

136286720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26166522-A-G

http://identifiers.org/hco/9/GRCh38#136286722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166524-C-A

136286753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26166560-G-A

http://identifiers.org/hco/9/GRCh38#136286793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26166598-C-A

136286793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26166598-C-T

http://identifiers.org/hco/9/GRCh38#136289888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26169880-C-A

136289888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26169880-C-T

http://identifiers.org/hco/9/GRCh38#136289910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26169898-C-A

136290016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26170001-A-G

136290249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26170216-G-A

136290308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26170319-C-T

136290448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26170462-G-A

136290448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26170462-G-T

136290513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26170518-G-A

136290513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26170518-G-C

136290513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26170518-G-T

136290550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26170555-A-G

136290603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26170608-C-T

136290606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26170611-G-A

136290606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26170611-G-T

136290608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26170613-T-C

136290636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26170641-G-T

136290667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26170672-G-A

136290667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26170672-G-T

136291127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171108-C-T

136291254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26171235-G-A

136291254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26171235-G-T

136291258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171239-G-A

136291258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171239-G-T

136291327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171311-G-A

136291400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26171390-G-A

136291400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171390-G-C

136291400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171390-G-T

136291414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171404-G-T

http://identifiers.org/hco/9/GRCh38#136291432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26171423-C-A

136291432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171423-C-G

136291432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171423-C-T

http://identifiers.org/hco/9/GRCh38#136291458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26171448-C-A

136291458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26171448-C-T

136291559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171549-C-G

136291559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171549-C-T

136291582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171572-G-A

136291619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26171609-T-C

136291665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26171664-A-G

136291853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26171866-C-T

136291968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26171966-G-A

136291968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26171966-G-C

http://identifiers.org/hco/9/GRCh38#136292051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26172025-C-A

136292051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26172025-C-T

136292112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26172075-C-T

http://identifiers.org/hco/9/GRCh38#136292129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26172092-C-A

136292129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26172092-C-T

136292273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26172217-G-A

136292273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 26172217-G-C

136292376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26172297-T-C

136295317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26176103-C-T

136295749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26176536-G-A

136295749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26176536-G-T

136297594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26177830-A-T

http://identifiers.org/hco/9/GRCh38#136297605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26177841-C-A

136297605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26177841-C-T

136297699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26177931-A-G

136297750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26177971-G-T

136297767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26177988-G-A

136297767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26177988-G-T

136297845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178063-G-A

136297845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178063-G-T

136298215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178145-G-C

136298238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178168-G-A

136298277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178205-G-A

136298368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178277-G-A

136299261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26178991-A-G

http://identifiers.org/hco/9/GRCh38#136299332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26179051-A-C

136299748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179394-A-T

136300019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179602-C-T

136300204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179694-C-T

136300224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26179714-A-G

136300248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26179738-G-A

http://identifiers.org/hco/9/GRCh38#136300275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26179765-C-A

136300327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179817-G-T

136300343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179835-G-A

136300343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179835-G-C

136300343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179835-G-T

136300418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179894-T-C

136300418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179894-T-G

136300434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179910-G-C

136300434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26179910-G-T

136302800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26183338-G-A

136302835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26183373-G-A

136302863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26183401-T-C

136302863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26183401-T-G

136303256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26183803-G-T

136303393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26183952-A-G

http://identifiers.org/hco/9/GRCh38#136303438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26183993-A-C

136303558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26184111-G-T

136303628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26184189-G-T

136303652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26184216-A-G

136303783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26184348-T-G

136303896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26184458-T-C

http://identifiers.org/hco/9/GRCh38#136303995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26184547-C-A

http://identifiers.org/hco/9/GRCh38#136304127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26184665-C-A

136304127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26184665-C-G

136304127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30942
most severe consequence: intron variant
orthologous variants: 26184665-C-T