3722683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34811894-C-G

3722723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34811934-G-A

3722740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34811953-A-G

3722775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34811997-G-A

3722925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812160-C-T

3722930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812163-G-A

http://identifiers.org/hco/6/GRCh38#3722946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812179-C-A

3722946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812179-C-G

3722955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812188-A-G

http://identifiers.org/hco/6/GRCh38#3722993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812218-C-A

3723022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812247-G-A

3723022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812247-G-C

3723081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812308-G-A

3723094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812321-G-C

3723094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812321-G-T

3723123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812347-T-A

3723142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812366-T-C

3723143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812367-G-A

3723143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812367-G-T

3723152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812376-A-T

3723224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812453-G-T

3723284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812490-G-C

3723286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812492-A-G

3723286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812492-A-T

3723325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812518-C-T

http://identifiers.org/hco/6/GRCh38#3723352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812537-C-A

3723352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812537-C-T

3723367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812555-G-A

http://identifiers.org/hco/6/GRCh38#3723373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812557-C-A

3723373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812557-C-T

3723390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812574-G-A

3723390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812574-G-T

3723446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812594-G-T

3723453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812601-C-T

http://identifiers.org/hco/6/GRCh38#3723473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812621-C-A

3723473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812621-C-T

3723550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812686-G-T

http://identifiers.org/hco/6/GRCh38#3723565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812700-C-A

3723608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812743-G-A

3723608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34812743-G-T

3723661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34812796-T-C

3723664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34812799-C-T

http://identifiers.org/hco/6/GRCh38#3723797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34812952-C-A

3723797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812952-C-T

http://identifiers.org/hco/6/GRCh38#3723827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34813026-C-A

3723827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813026-C-T

http://identifiers.org/hco/6/GRCh38#3723828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34813027-C-A

3723828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813027-C-T

3723841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813039-G-A

3723841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813039-G-T

http://identifiers.org/hco/6/GRCh38#3723851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34813050-C-A

3723851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813050-C-T

http://identifiers.org/hco/6/GRCh38#3723866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34813063-A-C

3723866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813063-A-G

3723883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813084-T-A

3723883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813084-T-C

3723883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813084-T-G

3723884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813085-G-A

3723884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813085-G-T

3724062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813230-C-T

3727894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815243-C-T

3727934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815282-T-C

3728464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815537-T-G

3728536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815610-T-C

3728935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816243-C-T

http://identifiers.org/hco/6/GRCh38#3729046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34816360-C-A

3729280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816602-C-T

http://identifiers.org/hco/6/GRCh38#3729306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34816630-C-A

3729477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816855-C-T

3729619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816988-G-A

3729619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816988-G-T

3729669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817032-G-A

3729965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817301-G-A

3730243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817536-C-T

3730244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817537-C-T

3730618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817930-C-T

3730620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817932-T-C

3731246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818587-C-G

3731273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818616-G-C

http://identifiers.org/hco/6/GRCh38#3731274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34818617-C-A

3731392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818743-A-T

3731406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818757-A-T

3731482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818832-G-A

3731552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819098-T-A

3731552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819098-T-C

http://identifiers.org/hco/6/GRCh38#3731555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34819101-A-C

3731564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819110-T-A

3731565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819111-T-C

3731603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819143-C-G

3731603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819143-C-T

3731690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819222-C-G

http://identifiers.org/hco/6/GRCh38#3731822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34819344-C-A

3731822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819344-C-T

http://identifiers.org/hco/6/GRCh38#3731864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34819392-C-A

3731864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819392-C-T

http://identifiers.org/hco/6/GRCh38#3731881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34819418-A-C

3731921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819461-T-C

3731922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819462-G-C

3732034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819538-T-C

3732352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819831-A-T

3732419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819899-A-G

3732490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819968-A-G

http://identifiers.org/hco/6/GRCh38#3732507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34819989-C-A

3732507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819989-C-T

3732800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820268-A-G

3732811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820271-T-C

3732935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820412-A-G

3732991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820468-G-C

3737032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822106-G-T

http://identifiers.org/hco/6/GRCh38#3737039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822113-C-A

3737039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822113-C-T

3737059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822128-G-A

3737059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822128-G-T

http://identifiers.org/hco/6/GRCh38#3737253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822321-C-A

3737253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822321-C-G

http://identifiers.org/hco/6/GRCh38#3737271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822330-C-A

3737307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822378-A-G

http://identifiers.org/hco/6/GRCh38#3737308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822379-C-A

3737308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822379-C-T

3737309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822380-G-A

3737309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822380-G-T

3737320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822391-G-A

3737320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822391-G-T

http://identifiers.org/hco/6/GRCh38#3737333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822406-C-A

3737333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822406-C-T

3737340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822414-G-A

3737340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822414-G-T

3737466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822527-T-C

3737537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822586-C-G

3737635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34822669-G-A

3737650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34822682-C-T

3737775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822790-T-C

3737780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822795-A-G

3737780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822795-A-T

3737798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822815-C-T

3737803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822820-C-T

3737816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822829-C-T

3737823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822837-T-C

3737823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822837-T-G

3737851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822861-G-A

3737852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822862-G-A

3737867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822877-T-A

http://identifiers.org/hco/6/GRCh38#3737869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822879-C-A

http://identifiers.org/hco/6/GRCh38#3737911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34822894-C-A

3737911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822894-C-T

3737917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822903-G-T

3737959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822936-A-G

3737966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822938-T-A

3738003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822962-G-A

3738003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822962-G-T

3738006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822965-G-A

3738006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822965-G-T

3738010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822969-C-T

http://identifiers.org/hco/6/GRCh38#3738188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34823127-A-C

3738191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823130-A-G

http://identifiers.org/hco/6/GRCh38#3738227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34823161-C-A

3738227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823161-C-G

3738404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823972-G-A

3738404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823972-G-C

3738476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824044-C-T

3738481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824049-C-T

http://identifiers.org/hco/6/GRCh38#3738682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34824230-A-C

3738682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824230-A-G

3738682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824230-A-T

http://identifiers.org/hco/6/GRCh38#3738687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34824233-A-C

3738687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824233-A-G

3738688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824234-G-C

3738688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824234-G-T

3738717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824263-A-G

3738728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824274-T-C

3738733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824279-T-C

http://identifiers.org/hco/6/GRCh38#3738735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34824281-C-A

3738735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824281-C-G

3738757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824317-G-C

3738757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824317-G-T

3738848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34824405-G-A

3738848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 34824405-G-T

3738850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34824407-A-G

3738909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34824462-G-A

3738980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34824530-T-C

3739198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824738-T-C

http://identifiers.org/hco/6/GRCh38#3739243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34824774-C-A

3739243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824774-C-T

http://identifiers.org/hco/6/GRCh38#3739245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34824776-A-C

http://identifiers.org/hco/6/GRCh38#3739261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34824793-C-A

3739267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824799-T-A

3739275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824807-A-G

3739275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824807-A-T

3739292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824849-C-T

3739537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825233-G-A

http://identifiers.org/hco/6/GRCh38#3739542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34825238-A-C

3739560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825256-G-T

3739666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825361-C-T

3739705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825381-A-G

http://identifiers.org/hco/6/GRCh38#3739732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34825404-A-C

3739925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825781-T-C

3740153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826011-G-A

3742350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826749-T-C

http://identifiers.org/hco/6/GRCh38#3742353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34826752-A-C

3742353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826752-A-G

3742401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826800-G-T

3742406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826805-T-C

3742450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34827000-C-T

http://identifiers.org/hco/6/GRCh38#3742657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#34827219-C-A

3742666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34827228-T-G

3742717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34827282-C-G

3743151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34827801-T-C

3743170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34827858-G-A

3743180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34827868-C-T

3743414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828084-T-A

3743504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828187-G-A

3743738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828478-T-A

3743743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828483-C-T

3743748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828491-T-C

3743766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828508-G-A

3743832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828570-C-T

3743869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828602-T-C

3743880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828609-T-G

3743882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828611-A-G

3743979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828765-G-A

http://identifiers.org/hco/6/GRCh38#3744072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34828875-C-A

3744072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828875-C-G

3744094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34828896-C-T

3744304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829235-A-G

3744321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829287-G-A

3744354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829325-T-G

http://identifiers.org/hco/6/GRCh38#3744457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34829413-C-A

3744457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829413-C-G

3744529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829482-T-G

3744547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829498-G-A

3744554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829505-G-C

3744554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829505-G-T

3744640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829558-C-T

http://identifiers.org/hco/6/GRCh38#3746192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34831456-A-C

3746292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34831568-A-G

http://identifiers.org/hco/6/GRCh38#3746433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34831691-C-A

3746583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34831833-T-C

3746599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34831848-G-A

3746728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34831947-G-A

3746828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832026-T-C

3746858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832062-C-T

3746939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832125-G-A

3746975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832145-G-A

3747035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832204-G-A

3747075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832245-G-T

http://identifiers.org/hco/6/GRCh38#3747076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34832246-C-A

3747232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832352-C-T

3747234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832354-C-G

3747265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832386-G-A

3747265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832386-G-T

3747385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832527-G-A

3747431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832574-A-G

http://identifiers.org/hco/6/GRCh38#3747522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34832664-C-A

3747997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833046-T-C

3748077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833132-G-T

http://identifiers.org/hco/6/GRCh38#3748386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34833482-A-C

3748403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34833498-C-G

3748421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833516-C-G

http://identifiers.org/hco/6/GRCh38#3748625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34833674-A-C

3748677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34833727-C-T

3748906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833900-C-T

3748929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833923-T-C

3749043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834035-A-G

3749057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834049-G-C

3749134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834115-C-T

3749189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834172-C-T

3749251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834265-C-T

3749287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834283-G-A

http://identifiers.org/hco/6/GRCh38#3749321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34834309-C-A

3749321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834309-C-T

3749356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834343-C-T

3749409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834391-C-T

3749717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834683-C-T

3749862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834807-A-T

3749868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834813-G-A

3749868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834813-G-C

3749884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34834829-T-C

3750081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835001-G-C

3750081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835001-G-T

3750084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835004-C-G

3750084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835004-C-T

3750340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835246-T-C

3750340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835246-T-G

3750370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835278-G-T

3750372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835280-G-A

3750438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835329-G-A

3750438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835329-G-T

http://identifiers.org/hco/6/GRCh38#3750465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34835356-A-C

3750502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34835385-C-T

3750677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835540-G-A

3750800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835680-G-C

3750813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835693-G-C

3750847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835729-C-G

3750939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835803-G-A

3750966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835831-G-A

3750966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835831-G-T

http://identifiers.org/hco/6/GRCh38#3750991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34835855-C-A

3750991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835855-C-G

3751070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34835936-C-T

http://identifiers.org/hco/6/GRCh38#3751091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34835955-C-A

3751091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34835955-C-T

3751186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34836061-G-A

3751186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34836061-G-T

http://identifiers.org/hco/6/GRCh38#3751246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#34836126-C-A

3751246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34836126-C-T

http://identifiers.org/hco/6/GRCh38#3751291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34836178-C-A

3751291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34836178-C-T

3751355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34836242-G-A

3751355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34836242-G-T

3751466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34836353-G-A

3751580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836477-G-A

3751580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836477-G-T

3751614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836510-C-T

3751637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836550-G-A

3751637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836550-G-T

http://identifiers.org/hco/6/GRCh38#3751646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#34836579-C-A

3751646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836579-C-G

3751646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836579-C-T

3751676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836631-G-A

3751676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21361
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34836631-G-T